Yellow nail syndrome in anti-SSA and anti-SSB positive primary Sjogren's syndrome

被引：0

作者：

D'Adamo, Laura Jayne ^{[1
]}

Oh, Yumi ^{[2
,3
]}

Young, Laurel ^{[2
,3
]}

机构：

[1] Royal Brisbane & Womens Hosp, Dept Internal Med, Brisbane, QLD, Australia

[2] Redcliffe Hosp, Dept Rheumatol, Brisbane, QLD, Australia

[3] Redcliffe Northside Rheumatol, Brisbane, QLD, Australia

来源：

BMJ CASE REPORTS | 2024年 / 17卷 / 08期

关键词：

Sjogren's syndrome; Rheumatology; INTESTINAL LYMPHANGIECTASIA; RHEUMATOID-ARTHRITIS; LYMPHEDEMA;

D O I：

10.1136/bcr-2024-260614

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Yellow nail syndrome (YNS) is a rare, acquired condition, characterised by at least two of the three clinical criteria: nail changes, respiratory tract disease and lymphoedema. Currently, the aetiology of YNS remains unknown; however, it is believed to be caused by impaired lymphatic drainage. Currently, there remain no definitive treatment options available and no prospective trials evaluating this. Management includes supportive care and symptomatic treatment. The presence of YNS has been described alongside various conditions, including autoimmune diseases, malignancies and drug exposures. To strengthen the literature on this topic, we present the case of a female patient with a history of anti-SSA and anti-SSB positive primary Sjogren's syndrome, who developed YNS in the immediate postpartum period.

引用

页码：1 / 4

页数：4